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Benzoic acid, 2-(1H-indol-3-ylcarbonyl)-, methyl ester is a chemical compound with the molecular formula C12H9NO3. It is a derivative of benzoic acid, featuring an indole-3-carbonyl group attached to the 2-position of the benzene ring and a methyl ester group at the carboxylic acid position. Benzoic acid, 2-(1H-indol-3-ylcarbonyl)-, methyl ester is known for its potential applications in pharmaceuticals and as an intermediate in the synthesis of various organic compounds. It is characterized by its ability to form a zwitterion, which is a molecule that has both a positive and a negative charge. The compound is typically synthesized through a Fischer indole reaction, a method used to form the indole nucleus. It is an important building block in the creation of various indole-based compounds, which are prevalent in natural products and have diverse biological activities.

6243-59-0

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6243-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6243-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6243-59:
(6*6)+(5*2)+(4*4)+(3*3)+(2*5)+(1*9)=90
90 % 10 = 0
So 6243-59-0 is a valid CAS Registry Number.

6243-59-0Relevant academic research and scientific papers

ARYL HYDROCARBON RECEPTOR MODULATORS AND USES THEREOF

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Paragraph 00426; 00450, (2019/10/29)

Provided are compounds of Formula (I), and pharmaceutically acceptable salts, solvates, hydrates, stereoisomers, tautomers, isotopically labeled derivatives, polymorphs, and prodrugs thereof, wherein X1-X4, RX, RC, RB, n, and Ring A are as defined herein. The compounds may be aryl hydrocarbon receptor agonists or partial aryl hydrocarbon receptor agonists. Also provided are pharmaceutical compositions comprising a compound of Formula (I) and methods of using such compounds for treating diseases and conditions related to the activity of an aryl hydrocarbon receptor, such as, for example, inflammatory diseases, autoimmune diseases, metabolic disorders, and proliferative diseases.

A Novel Total Synthesis of Indolo[2,3-b]naphthalene-6,11-diones

Fernandez, Marcos,Barcia, Carlos,Estévez, Juan C.,Estévez, Ramón J.,Castedo, Luis

, p. 267 - 270 (2007/10/03)

A new total synthesis of indolo[2,3-b]naphthalene-6,11-diones is described, which involves a novel opening of 2-(2′-nitrophenyl)-2-methoxycarbonyl-1- indanones to 2-[2-memoxycarbonyl-2-(2-nitrophenyl)ethyl]benzoic acids followed by a two-steps transformat

Synthesis, electrochemistry, and bioactivity of the cyanobacterial calothrixins and related quinones

Bernardo, Paul H.,Chai, Christina L. L.,Heath, Graham A.,Mahon, Peter J.,Smith, Geoffrey D.,Waring, Paul,Wilkes, Bronwyn A.

, p. 4958 - 4963 (2007/10/03)

The calothrixins are quinone-based natural products isolated from Calothrix cyanobacteria which show potent antiproliferative properties against several cancer cell lines. Preliminary mechanistic studies suggest that the biological mode of action of the c

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